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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161975Generated: October 29, 2026

Ammonia → 11beta-Methyl 17beta-hydroxyestr-5(10)-en-3-one

https://huagongshe.com/reaction/1161975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttert-ButanolHCID 6386—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithiumHCID 3028194—
ReactantLithium ammoniaHCID 57431548—
Reactant11beta-Methyl-17beta-hydroxyestra-4,9-dieneHCID 68648355—
SolventTetrahydrofuranHCID 8028—
Product11beta-Methyl 17beta-hydroxyestr-5(10)-en-3-oneHCID 86621277100%

Reaction Steps

Under an argon atmosphere, lithium wire (270 mg, 38.9 mmol), cut into small pieces, was added to anhydrous ammonia (200 mL) and stirred at reflux for 2 hr. The lithium/ammonia mixture was chilled to −78° C. and a THF solution of the dienone (5a, 4.03 g, 14.07 mmol) containing t-butanol (1.24 mL), was added over 15 min. The mixture was stirred at −78° C. for 15 min before excess of lithium was destroyed with isoprene (1.5 mL). The reaction was quenched by means of the addition of solid ammonium chloride (16 g, 296.3 mmol). Ammonia was allowed to evaporate under a constant stream of nitrogen. The THF layer was washed with H2O and brine. The aqueous washes were extracted with ether (2×200 mL). the combined organic extracts were dried over Na2SO4 and evaporation of the solvent gave 4.25 g of 6a as a white solid in 100% yield. NMR (300 MHz, CDCl3): δ 0.889 (s, 3H, C18-7CH3), 0.916 (d, 3H, C11β-CH3), and 3.655 (t, 1H, C17β-H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820642B2
Source datasetuspto-grants-2010_10
ORD IDord-a8f3622d17454de88e89e3f6d72195e8
Source noteuspto-grants-2010_10